Ic. Solomon et al., Patterns of phrenic motor output evoked by chemical stimulation of neuronslocated in the pre-Botzinger complex in vivo, J NEUROPHYS, 81(3), 1999, pp. 1150-1161
The pre-Botzinger complex (pre-BotC) has been proposed to be essential for
respiratory rhythm generation from work in vitro. Much less, however, is kn
own about its role in the generation and modulation of respiratory rhythm i
n vivo. Therefore we examined whether chemical stimulation of the in vivo p
re-BotC manifests respiratory modulation consistent with a respiratory rhyt
hm generator. In chloralose- or chloralose/urethan-anesthetized, vagotomize
d cats, we recorded phrenic nerve discharge and arterial blood pressure in
response to chemical stimulation of neurons located in the pre-BotC with DL
-homocysteic acid (DLH; 10 mM; 21 nl). In 115 of the 122 sites examined in
the pre-BotC, unilateral microinjection of DLH produced an increase in phre
nic nerve discharge that was characterized by one of the following changes
in cycle timing and pattern: 1) a rapid series of high-amplitude, rapid rat
e of rise, short-duration bursts, 2) tonic excitation (with or without resp
iratory oscillations), 3) an integration of the first two types of response
s (i.e., tonic excitation with high-amplitude, short-duration bursts superi
mposed), or 4) augmented bursts in the phrenic neurogram (i.e., eupneic bre
ath ending with a high-amplitude, short-duration burst). In 107 of these si
tes, the phonic neurogram response was accompanied by an increase or decrea
se (greater than or equal to 10 mmHg) in arterial blood pressure. Thus incr
eases in respiratory burst frequency and production of tonic discharge of i
nspiratory output, both of which have been seen in vitro, as well as modula
tion of burst pattern can be produced by local perturbations of excitatory
amino acid neurotransmission in the preBotC in vivo. These findings are con
sistent with the proposed role of this region as the locus for respiratory
rhythm generation.